Method for reducing damage by harmful organisms in corn cultivation

ABSTRACT

Provided is a method for reducing damage by harmful organisms in corn cultivation. Damage by harmful organisms in corn cultivation can be reduced by carrying out the steps of: A) making a furrow in a cultivated land; B) seeding the furrow formed in the foregoing step with corn; C) applying to the furrow one or more selected from Compound Group (II), or C′) applying to the furrow one or more selected from Compound Group (I) and one or more selected from Compound Group (II); and D) closing the furrow. Compound Group (I): clothianidin, thiamethoxam, imidacloprid and thiacloprid; Compound Group (II): bifenthrin, bioresmethrin, deltamethrin, bioallethrin, ethofenprox, fenpropathrin, cypermethrin, alpha-cypermethrin, zeta-cypermethrin, fenvalerate, esfenvalerate, cyfluthrin, beta-cyfluthrin, alpha-cypermethrin, tralomethrin, fluvalinate, permethrin, lambda-cyhalothrin, flucythrinate and tefluthrin.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a Divisional of co-pending application Ser. No.13/944,367 filed on Jul. 17, 2013, which claims priority under 35 U.S.C.§119(a) to Patent Application No. 2012-161340 filed in Japan on Jul. 20,2012. All of the above applications are hereby expressly incorporated byreference into the present application.

BACKGROUND OF THE INVENTION

Field of the Invention

The present invention relates to a method for reducing damage by harmfulorganisms in corn cultivation.

Description of the Related Art

Previously, various methods have been known as a method for reducingdamage by harmful organisms in corn cultivation.

PRIOR ART LITERATURE Non-Patent Literature

-   Non-Patent Literature 1: Handbook of Corn Insects. ISBN:    0-938522-76-0., 1999. Entomological Society of America

SUMMARY OF THE INVENTION

In corn cultivation, with worldwide cereal demand expansion, variousefforts have been made in order to increase a yield, but since areduction in yield due to harmful organisms such as pests and weeds hasbeen significant, development of a method for reducing damage by harmfulorganisms in corn cultivation has been desired.

The present inventors have conducted studies for finding out a methodfor reducing damage by harmful organisms in corn cultivation, andresultantly found out that damage by harmful organisms in corncultivation can be reduced by carrying out the steps of: A) making afurrow in a cultivated land (hereinafter, referred to as step A in somecases); B) seeding with corn a furrow formed in the foregoing step(hereinafter, referred to as step B in some cases); C) applying to thefurrow one or more selected from the below-mentioned compound group (II)(hereinafter, referred to as the present compound (II) in some cases)(hereinafter, referred to as step C in some cases); and D) closing thefurrow (hereinafter, referred to as step D in some cases).

The present inventors have also conducted studies for finding out amethod for reducing damage by harmful organisms in corn cultivation, andresultantly found out that damage by harmful organisms in corncultivation can be reduced by carrying out the steps of: A) making afurrow in a cultivated land (hereinafter, referred to as step A in somecases); B) seeding with corn a furrow formed in the foregoing step(hereinafter, referred to as step B in some cases); C′) applying to thefurrow one or more selected from the below-mentioned compound group (I)(hereinafter, referred to as the present compound (I) in some cases) andone or more selected from the below-mentioned compound group (II)(hereinafter, referred to as the present compound (II) in some cases)(hereinafter, referred to as step C′ in some cases); and D) closing thefurrow (hereinafter, referred to as step D in some cases).

That is, the present invention is as follows:

[1] A method for reducing damage by harmful organisms in corncultivation, the method comprising the steps of:

A) making furrow in a cultivated land; B) seeding with corn a furrowformed in the foregoing step; C) applying to the furrow one or moreselected from the below-mentioned compound group (II); and D) closingthe furrow.(compound group (II): group consisting of bifenthrin, bioresmethrin,deltamethrin, bioallethrin, ethofenprox, fenpropathrin, cypermethrin,alpha-cypermethrin, zeta-cypermethrin, fenvalerate, esfenvalerate,cyfluthrin, beta-cyfluthrin, alpha-cypermethrin, tralomethrin,fluvalinate, permethrin, lambda-cyhalothrin, flucythrinate andtefluthrin)

[2] The method according to [1], wherein the step of applying one ormore selected from the compound group (II) is a step of applying acomposition containing one or more selected from the compound group(II).

[3] The method according to [2], wherein the composition containing oneor more selected from the compound group (II) is a granule ormicro-granule containing one or more selected from the compound group(II).

[4] The method according to [2], wherein the composition containing oneor more selected from the compound group (II) is an aqueous dispersionor aqueous solution containing one or more selected from the compoundgroup (II).

[5] The method according [4], wherein the aqueous dispersion or aqueoussolution is an aqueous dispersion or aqueous solution obtained bydispersing or dissolving in water a water soluble powder, a wettablepowder, a water dispersible granule, a soluble concentrate, amicrocapsule, an emulsifiable concentrate, a concentrated emulsion, amicroemulsion, a suspoemulsion, an oil miscible liquid, a suspensionconcentrate or a dry flowable which contains one or more selected fromthe compound group (II).

[6] A method for reducing damage by harmful organisms in corncultivation, the method including the steps of:

A) making a furrow in a cultivated land; B) seeding with corn a furrowformed in the foregoing step; C′) applying to the furrow one or moreselected from the below-mentioned compound group (I) and one or moreselected from the below-mentioned compound group (II); and D) closingthe furrow. (compound group (I): group consisting of clothianidin,thiamethoxam, imidacloprid and thiacloprid;compound group (II): group consisting of bifenthrin, bioresmethrin,deltamethrin, bioallethrin, ethofenprox, fenpropathrin, cypermethrin,alpha-cypermethrin, zeta-cypermethrin, fenvalerate, esfenvalerate,cyfluthrin, beta-cyfluthrin, alpha-cypermethrin, tralomethrin,fluvalinate, permethrin, lambda-cyhalothrin, flucythrinate andtefluthrin)

[7] The method according to [6], wherein the step of applying one ormore selected from the compound group (I) and one or more selected fromthe compound group (II) is a step of applying a composition containingone or more selected from the compound group (I) and a compositioncontaining one or more selected from the compound group (II).

[8] The method according to [7], wherein the composition containing oneor more selected from the compound group (I) is a granule ormicro-granule containing one or more selected from the compound group(I).

[9] The method according to [7], wherein the composition containing oneor more selected from the compound group (I) is an aqueous dispersion oraqueous solution containing one or more selected from the compound group(I).

[10] The method according to any one of [7] to [9], wherein thecomposition containing one or more selected from the compound group (II)is a granule or micro-granule containing one or more selected from thecompound group (II).

[11] The method according to any one of [7] to [9], wherein thecomposition containing one or more selected from the compound group (II)is an aqueous dispersion or aqueous solution containing one or moreselected from the compound group (II).

[12] The method according to [9], wherein the aqueous dispersion oraqueous solution is an aqueous dispersion or aqueous solution obtainedby dispersing or dissolving in water a water soluble powder, a wettablepowder, a water dispersible granule, a soluble concentrate, amicrocapsule, an emulsifiable concentrate, a concentrated emulsion, amicroemulsion, a suspoemulsion, an oil miscible liquid, a suspensionconcentrate or a dry flowable which contains one or more selected fromthe compound group (I).

[13] The method according to [11], wherein the aqueous dispersion oraqueous solution is an aqueous dispersion or aqueous solution obtainedby dispersing or dissolving in water a water soluble powder, a wettablepowder, a water dispersible granule, a soluble concentrate, amicrocapsule, an emulsifiable concentrate, a concentrated emulsion, amicroemulsion, a suspoemulsion, an oil miscible liquid, a suspensionconcentrate or a dry flowable which contains one or more selected fromthe compound group (II).

[14] The method according to [6], wherein the step of applying one ormore selected from the compound group (I) and one or more selected fromthe compound group (II) is a step of applying a composition containingone or more selected from the compound group (I) and one or moreselected from the compound group (II).

[15] The method according to [14], wherein the composition containingone or more selected from the compound group (I) and one or moreselected from the compound group (II) is a granule or micro-granulecontaining one or more selected from the compound group (I) and one ormore selected from the compound group (II).

[16] The method according to [14], wherein the composition containingone or more selected from the compound group (I) and one or moreselected from the compound group (II) is an aqueous dispersion oraqueous solution containing one or more selected from the compound group(I) and one or more selected from the compound group (II).

[17] The method according to [16], wherein the aqueous dispersion oraqueous solution is an aqueous dispersion or aqueous solution obtainedby dispersing or dissolving in water a water soluble powder, a wettablepowder, a water dispersible granule, a soluble concentrate, amicrocapsule, an emulsifiable concentrate, a concentrated emulsion, amicroemulsion, a suspoemulsion, an oil miscible liquid, a suspensionconcentrate or a dry flowable which contains one or more selected fromthe compound group (I) and one or more selected from the compound group(II).

[18] The method according to any one of [1] to [17], wherein the land isditched to a depth of 1 to 10 cm.

[19] The method according to any one of [1] to [18], wherein makingfurrow is performed using a disk furrow opener.

[20] The method according to any one of [1] to [19], wherein seeding isperformed using a pneumatic seeder.

According to the present invention, harmful organisms in corncultivation can be prevented, therefore, damage by harmful organisms incorn cultivation can be reduced.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

For the order of carrying out steps, usually, a step A, and then steps Band C or C′ are carried out. In the step A, usually, a furrow having aV-shaped cross section is formed in a linear shape on a cultivated land.The step A may be carried out, followed by carrying out the step B, andthen the step C or C′, or the order may be reversed. The steps B and Cor C′ may be carried out in parallel. Usually, a step D is carried outafter the steps B and C or C′.

In the present invention, usually, a seeder which is pulled with atractor is used. Examples of the seeder include a composite-type seederincluding a ditching part for forming a furrow, a seeding part forseeding a furrow in a speed linkage manner through piping from a hopperbox filled with a seed, an agricultural chemical application parts forapplying the present compound (II) or an agricultural chemicalapplication part for applying the present compound (I) and the presentcompound (II) aqueous solution in a speed linkage manner through pipingfrom one or more reservoirs filled with the present compound (I) and thepresent compound (II) collectively or separately, a furrow closing partfor closing the furrow by gathering together a soil on the side of theformed furrow, and so on.

The ditching part of a seeder is usually attached to a front part of theseeder, and a furrow is formed on a cultivated land with movement of atractor. Examples of the ditching part include a ploughshare furrowopener and a disk furrow opener, and a ditching system using a diskfurrow opener which has a strong force of cutting a crop residue, has asmall reduction in a cutting force due to adhesion of a soil, and canstabilize the depth of a furrow is preferable in that a furrow can beseeded and a chemical can be applied to the furrow uniformly due tostabilization of a depth of a furrow, so that the effect of the chemicalis stabilized.

The depth of the furrow formed on a cultivated land can be appropriatelychanged depending on the soil condition of a place of corn cultivation,the condition of cultivating corn thereafter, and the weather condition,and is usually 1 to 10 cm, preferably 2 to 8 cm, further preferably 2 to6 cm.

The seeding part of the seeder is usually attached to a rear of theditching part, and the furrow is seeded with movement of a tractor.Examples of the seeding part include a mechanical seeder and a pneumaticseeder, and the pneumatic seeder using air pressure is preferable inthat seed clogging or seeding leakage is small, so that seeding isstablyperformed, and a seed can be seeded in a furrow orderly. Examplesof the pneumatic seeder include a vacuum suction type seeder and ablowing type seeder, and based on the reason of imparting little damageto a seed, a vacuum suction type seeder is preferable.

In the present invention when the present compound (II) is used,tefluthrin, bifenthrin, esfenvalerate, fenpropathrin, lambda-cyhalothrinor alpha-cypermethrin is preferable as the present compound (II). In thepresent invention when the present compound (I) and the present compound(II) are used, clothianidin, thiamethoxam or imidacloprid is preferableas the present compound (I), and tefluthrin, bifenthrin, esfenvalerate,fenpropathrin, lambda-cyhalothrin or alpha-cypermethrin is preferable asthe present compound (II).

Clothianidin is a known compound, and is described in, for example, “ThePesticide Manual—15^(th) edition (published by BCPC); ISBN978-1-901396-18-8”, page 229. This compound is obtained from acommercially available preparation, or is obtained by production througha known method.

Thiamethoxam is a known compound, and is described in, for example, “ThePesticide Manual—15^(th) edition (published by BCPC); ISBN978-1-901396-18-8”. page 1112. This compound is obtained from acommercially available preparation, or is obtained by production througha known method.

Imidacloprid is a known compound, and is described in, for example, “ThePesticide Manual—15^(th) edition (published by BCPC); ISBN978-1-901396-18-8”, page 645. This compound is obtained from acommercially available preparation, or is obtained by production througha known method.

Thiacloprid is a known compound, and is described in, for example, “ThePesticide Manual—15^(th) edition (published by BCPC); ISBN978-1-901396-18-8”, page 1111. This compound is obtained from acommercially available preparation, or is obtained by production througha known method.

Tefluthrin is a known compound, and is described in, for example, “ThePesticide Manual—15^(th) edition (published by BCPC); ISBN978-1-901396-18-8”, page 1083. This compound is obtained from acommercially available preparation, or is obtained by production througha known method.

Bifenthrin is a known compound, and is described in, for example, “ThePesticide Manual—15^(th) edition (published by BCPC); ISBN978-1-901396-18-8”, page 1083. This compound is obtained from acommercially available preparation, or is obtained by production througha known method.

Esfenvalerate is a known compound, and is described in, for example,“The Pesticide Manual—15^(th) edition (published by BCPC); ISBN978-1-901396-18-8”, page 433. This compound is obtained from acommercially available preparation, or is obtained by production througha known method.

Fenpropathrin is a known compound, and is described in, for example,“The Pesticide Manual—15^(th) edition (published by BCPC); ISBN978-1-901396-18-8”, page 433. This compound is obtained from acommercially available preparation, or is obtained by production througha known method.

Lambda-cyhalothrin is a known compound, and is described in, forexample, “The Pesticide Manual—15^(th) edition (published by BCPC); ISBN978-1-901396-18-8”, page 272. This compound is obtained from acommercially available preparation, or is obtained by production througha known method.

Alpha-cypermethrin is a known compound, and is described in, forexample, “The Pesticide Manual—15^(th) edition (published by BCPC); ISBN978-1-901396-18-8”, page 277. This compound is obtained from acommercially available preparation, or is obtained by production througha known method.

Bioresmethrin is a known compound, and is described in, for example,“The Pesticide Manual—15^(th) edition (published by BCPC); ISBN978-1-901396-18-8”, page 110. This compound is obtained from acommercially available preparation, or is obtained by production througha known method.

Deltamethrin is a known compound, and is described in, for example, “ThePesticide Manual—15^(th) edition (published by BCPC); ISBN978-1-901396-18-8”, page 313. This compound is obtained from acommercially available preparation, or is obtained by production througha known method.

Bioallethrin is a known compound, and is described in, for example, “ThePesticide Manual—15^(th) edition (published by BCPC); ISBN978-1-901396-18-8”, page 107. This compound is obtained from acommercially available preparation, or is obtained by production througha known method.

Ethofenprox is a known compound, and is described in, for example, “ThePesticide Manual—15^(th) edition (published by BCPC); ISBN978-1-901396-18-8”, page 454. This compound is obtained from acommercially available preparation, or is obtained by production througha known method.

Cypermethrin is a known compound, and is described in, for example, “ThePesticide Manual—15^(th) edition (published by BCPC); ISBN978-1-901396-18-8”, page 277. This compound is obtained from acommercially available preparation, or is obtained by production througha known method.

Zeta-cypermethrin is a known compound, and is described in, for example,“The Pesticide Manual—15^(th) edition (published by BCPC); ISBN978-1-901396-18-8”, page 284. This compound is obtained from acommercially available preparation, or is obtained by production througha known method.

Fenvalerate is a known compound, and is described in, for example, “ThePesticide Manual—15^(th) edition (published by BCPC); ISBN978-1-901396-18-8”, page 494. This compound is obtained from acommercially available preparation, or is obtained by production througha known method.

Cyfluthrin is a known compound, and is described in, for example, “ThePesticide Manual—15^(th) edition (published by BCPC); ISBN978-1-901396-18-8”, page 263. This compound is obtained from acommercially available preparation, or is obtained by production througha known method.

Beta-cyfluthrin is a known compound, and is described in, for example,“The Pesticide Manual—15^(th) edition (published by BCPC); ISBN978-1-901396-18-8”, page 265. This compound is obtained from acommercially available preparation, or is obtained by production througha known method.

Alpha-cypermethrin is a known compound, and is described in, forexample, “The Pesticide Manual—15^(th) edition (published by BCPC); ISBN978-1-901396-18-8”, page 279. This compound is obtained from acommercially available preparation, or is obtained by production througha known method.

Tralomethrin is a known compound, and is described in, for example, “ThePesticide Manual—15^(th) edition (published by BCPC); ISBN978-1-901396-18-8”, page 1142. This compound is obtained from acommercially available preparation, or is obtained by production througha known method.

Fluvalinate is a known compound, and is described in, for example, “ThePesticide Manual—15^(th) edition (published by BCPC); ISBN978-1-901396-18-8”, page 1236. This compound is obtained from acommercially available preparation, or is obtained by production througha known method.

Permethrin is a known compound, and is described in, for example, “ThePesticide Manual—15^(th) edition (published by BCPC); ISBN978-1-901396-18-8”, page 879. This compound is obtained from acommercially available preparation, or is obtained by production througha known method.

Flucythrinate is a known compound, and is described in, for example,“The Pesticide Manual—15^(th) edition (published by BCPC); ISBN978-1-901396-18-8”, page 519. This compound is obtained from acommercially available preparation, or is obtained by production througha known method.

The present compound (I) for use in the present invention may be thepresent composition (I) itself, but is usually formulated into anarbitrary dosage form such as a granule, a water soluble powder, awettable powder, a water dispersible granule, a soluble concentrate, amicrocapsule, an emulsifiable concentrate, a concentrated emulsion, amicroemulsion, a suspoemulsion, an oil miscible liquid, a suspensionconcentrate or a dry flowable by mixing the present compound (I) with anappropriate solid carrier or liquid carrier, and adding a surfactant andother formulation additives for a preparation as necessary.

Like the present compound (I), the present compound (II) may be thecompound (II) itself, but is usually formulated and used.

In the present invention, a formulation containing the present compound(II), or a formulation containing the present compound (I) and thepresent compound (II) (hereinafter, referred to as the presentformulation in some cases) may be used, or a formulation containing thepresent compound (I) (hereinafter, referred to as the presentformulation (I) in some cases) and a formulation containing the presentcompound (II) (hereinafter, referred to as the present formulation (II)in some cases) may be used in combination.

In the present invention, when the present formulation (I) and thepresent formulation (II) are used in combination, the presentformulation (I) and the present formulation (II) may be usedindividually, or may be mixed and used. The dosage forms of the presentformulation (I) and the present formulation (II) may be the same, or maybe different.

Examples of the solid carrier used upon formulation into a preparationinclude natural or synthetic minerals such as clay, kaolin, talc,bentonite, sericite, sulfur, active carbon, calcium carbonate,diatomaceous earth, quartz, pumice stone, calcite, meerschaum, dolomite,olivine, pyroxene, amphibole, feldspar, silica, alumina, vermiculite,and perlite; and fine grains of an elastomer, a plastic, a ceramic, ametal, sawdust, corncob, a kernel shell of coconut, a stem of tobaccoand the like.

Examples of the liquid carrier include water, xylene, methanol, butanol,pentanol, benzyl alcohol, cyclohexanon, gamma-butyrolactone,N-methyl-pyrrolidone, N-octyl-pyrrolidone, glycoldiacetate, glycols,fatty acid dimethylamides, fatty acids and fatty acid esters. They maybe mixed and used.

Examples of the surfactant include common nonionic surfactants, cationicsurfactants, anionic surfactants and amphoteric surfactants, and onekind or two or more kinds thereof are used.

Examples of the surfactant include an alkylsulfuric acid salt, analkylsulfuric acid ester salt, an alkylsulfonic acid salt, analkylarylsulfonic acid salt, a lignosulfonic acid ester, anaphthalenesulfonic acid salt, a phenolsulfonic acid salt, adibutylnaphthalenesulfonic acid salt, a fatty alcohol sulfuric acidsalt, fatty acid alkyl aryl ethers and polyoxyethylene compoundsthereof, polyethylene glycol ethers, polyethylene glycol fatty acidesters, polyhydric alcohol esters, a sugar alcohol derivative and asilicone-based surfactant.

Examples of the other formulation additives for a preparation include anemulsifier, a dispersant, an antifoamer, a stabilizer, an antiseptic anda colorant.

Examples of the preferred emulsifier include a nonionic emulsifier andan anionic emulsifier (e.g. a polyoxyethylene fatty alcohol ether, analkyl sulfonate and an aryl sulfonate). Examples of the dispersantinclude a lignin sulfurous acid waste liquid and methyl cellulose.

Examples of the preferred antifoamer include a silicone or magnesiumstearate-based antifoamer.

Examples of the colorant include red dyes, blue dyes, green dyes andyellow dyes and the like. Specific examples include Monazole Red,Cyanine Green, Prussian Blue and Brilliant Blue. Particularly, in thecase of a granule, it is preferable to add a colorant because thegranule is easily identified at the time of application or afterapplication.

Further, for example, glycerin, ethylene glycol and propylene glycol maybe added as an antifreezing agent.

When a granule is used in the step C or C′ of the present invention, itis applied as such without being diluted.

The granule can be a form such as a fine granule, a macro granule, or amicro granule, by changing the particle size thereof.

In the present invention in which the present compound (II) is used, thecontent of the present compound (II) in the granule is usually 0.01 to20% by weight, preferably 0.05 to 10% by weight, further preferably 0.1to 5% by weight. In the present invention in which the present compound(I) and the present compound (II) are used, the content of each of thepresent compound (I) and the present compound (II) in the granule isusually 0.01 to 20% by weight, preferably 0.05 to 10% by weight, furtherpreferably 0.1 to 5% by weight.

When a water soluble powder, a wettable powder, a water dispersiblegranule, a soluble concentrate, a microcapsule, an emulsifiableconcentrate, a concentrated emulsion, a microemulsion, a suspoemulsion,an oil miscible liquid, a suspension concentrate or a dry flowable isused in the step C or C′ of the present invention, an aqueous dispersionor aqueous solution obtained by dispersing or dissolving any of theaforementioned formulations in water is usually applied. The aqueousdispersion or aqueous solution may contain a herbicide, a safener andthe like.

The aqueous dispersion of the present compound (I) in the presentinvention includes a liquid formed by suspending the present compound(I) in water in a solid state, and a liquid formed by emulsifying thepresent compound (I) in water in a liquid state. The same holds true forthe aqueous dispersion of the present compound (II).

In the present invention in which the present compound (II) is used, theapplication amount of the present compound (II) can be appropriatelychanged depending on the condition of cultivating corn thereafter andthe weather condition, and is usually 5 to 500 g, preferably 10 to 400g, further preferably 10 to 200 g per hectare of a cultivated land whichis seeded with corn. In the present invention in which the presentcompound (I) and the present compound (II) are used, the applicationamount of each of the present compound (I) and the compound (II) can beappropriately changed depending on the condition of cultivating cornthereafter and the weather condition, and is usually 5 to 500 g,preferably 10 to 400 g, further preferably 10 to 200 g per hectare of acultivated land which is seeded with corn.

In the present invention in which the present compound (I) and thepresent compound (II) are used, the ratio of the application amounts ofthe present compound (I) and the present compound (II) in the presentinvention is usually 40:1 to 1:40, preferably 20:1 to 1:20 in terms of aweight ratio.

Usually, the present compound (II), or the present compound (I) and thepresent compound (II) is/are stored in a tank attached to a tractor bodyor a seeder pulled with a tractor, and is applied, in linkage with orindependently of a vehicle speed, through piping from the tank withmovement of the tractor.

In the step C, a granule or micro-granule containing the presentcompound (II) may be applied before or after seeding, but is preferablyapplied before seeding, and an aqueous dispersion or aqueous solution ofthe present compound (II) may be applied before or after seeding, but ispreferably applied in parallel to seeding or after seeding, so that theaqueous dispersion or aqueous solution of the present compound (II) isin direct contact with the seed.

When a granule or micro-granule containing the present compound (I) oran aqueous dispersion or aqueous solution of the present compound (II)is used in the step C′, the present compound (I) and the presentcompound (II) are both applied into the furrow, but usually the presentcompound (I) and the present compound (II) are stored separately in tworeservoirs, and each applied into the furrow. The granule ormicro-granule containing the present compound (I) may be applied beforeor after seeding, but is preferably applied before seeding. The aqueousdispersion or aqueous solution of the present compound (II) may beapplied before or after seeding, but is preferably applied in parallelto seeding or after seeding, so that the aqueous dispersion or aqueoussolution of the present compound (II) is in direct contact with theseed. When the present compound (I) and the present compound (II) arestored separately in two chemical tanks, positions of chemical nozzlesare adjusted to perform application orderly so that the compounds do notinterfere with each other during application.

Application is performed by a similar operation when the aqueousdispersion or aqueous solution of the present compound (I) and thegranule or micro-granule containing the present compound (II) areapplied.

When the aqueous dispersion or aqueous solution of the present compound(II), or the aqueous dispersion or aqueous solution of the presentcompound (I) and the present compound (II) is applied, the type ofapplication is not particularly limited as long as it is capable ofapplication into a furrow, but particularly spraying, dripping ordrenching is preferable.

When the type of application is spraying, dripping or drenching, byapplying a pressure with a pump or adjusting the opening of a valve of atank or a hose, the application amount can be adjusted to performuniform application to a furrow.

The furrow closing part is usually made of rubber or made of cast iron,has a wheel shape, and closes a furrow by gathering together on the sideof the furrow with movement of a tractor.

The present invention can reduce damage by harmful organisms in corncultivation.

In the present invention, the harmful organism refers to pests, weedsand the like.

Specific examples of insect pests which can be controlled by the presentinvention include insect pests belonging to Agriotes spp., Diabroticaspp., Agrotis spp., Myzus spp., Aphis spp., Ostrinia spp., Zyginidiaspp., Sesamia spp., Oscinella spp., Sitobion spp., Scutigerella spp.,Astylus spp., Rhopalosiphum spp., Metopolophium spp., Melanotus spp. andMelolontha spp., and the present invention is preferably applied as amethod for reducing damage by particularly Agriotes spp., Diabroticaspp., Agrotis spp. and Rhopalosiphum spp.

The variety of corn, to which the present invention can be applied, isnot particularly limited, but application of corn to a hybrid variety ispreferable. The hybrid variety is first cross obtained by mating twodifferent type of varieties, and generally has more excellentcharacteristics than those of both parents.

Corn may be corn to which resistance has been imparted by a geneticengineering technique or a breeding method by mating.

The corn seed used in the present invention is preferably treated with afungicide, and examples of the fungicide include fludioxonil, metalaxyl,metalaxyl-M, thiuram, triticonazole, carboxin, prochloraz,prothioconazole, sedaxane, penflufen, fluxapyroxad, trifloxystrobin,pyraclostrobin and difenoconazole, and fludioxonil, metalaxyl-M,thiuram, triticonazole, sedaxane, penflufen, and fluxapyroxad arepreferable, and fludioxonil, metalaxyl-M and thiuram are morepreferable. The corn seed is used after treated with one or more kindsof these fungicides. Alternatively, a commercially available treatedseed may be purchased and used.

It is preferable to apply a herbicide to a cultivated land before orafter seeding of corn in order to suppress generation of weeds during acultivation term of corn, and examples of the herbicide includemesotrione, nicosulfuron, S-metolachlor, acetochlor, terbuthylazine,sulcotrione, isoxaflutole, bromoxynil, dicamba, foramsulfuron,dimethenamid-P, rimsulfuron, bentazon, glyphosate, tembotrione,pendimethalin, flufenacet, fluroxypyr, pethoxamid, flumioxazin,thiencarbazone-methyl, iodosulfuron-methyl-sodium salt, prosulfuron,topramezone, metosulam, cycloxydim, aclonifen, dimethenamid, florasulam,clopyralid, flazasulfuron, imazamox, MCPA, 2,4-D, linuron, propisochlor,thifensulfuron methyl and tritosulfuron; preferably mesotrione,nicosulfuron, S-metolachlor, acetochlor, terbuthylazine, sulcotrione,isoxaflutole, bromoxynil, dicamba, foramsulfuron, dimethenamid-P,rimsulfuron, bentazon, glyphosate, tembotrione, pendimethalin,flufenacet, fluroxypyr, pethoxamid, flumioxazin, thiencarbazone-methyl,iodosulfuron-methyl-sodium salt, prosulfuron, topramezone, metosulam,cycloxydim and aclonifen; more preferably mesotrione, nicosulfuron,S-metolachlor, acetochlor, terbuthylazine, sulcotrione, isoxaflutole,bromoxynil, dicamba, foramsulfuron, dimethenamid-P, rimsulfuron,bentazon, glyphosate, tembotrione, pendimethalin, flufenacet,fluroxypyr, pethoxamid, flumioxazin, thiencarbazone-methyl andiodosulfuron-methyl-sodium salt. Usually, one or more of theseherbicides are applied. When two or more thereof are applied, they maybe applied simultaneously, or they may be applied separately. When theyare applied separately, they may be applied on the same day, or onanother day.

These herbicides may be applied by, if necessary, mixing with a safener.Examples of the safener include isoxadifen-ethyl, furilazole,dichlormid, benoxacor and cyprosulfamide.

EXAMPLES

Next the present invention will be further described byway of thefollowing examples, but the present invention is not limited to theseexamples.

Example 1

A land was ditched at intervals of 75 cm to a depth of 3 cm from thesoil surface, a predetermined amount of a mixed liquid of awater-diluted liquid of a clothianidin water disperscible granule (usinga 50% water disperscible granule, trade name: DANTOP, manufactured byPhilagro) and a water-diluted liquid of an esfenvalerate emulsifiableconcentrate (using 50 g/L of an EC preparation, trade name: Sumialpha5EC, manufactured by Philagro) or a mixed liquid of a water-dilutedliquid of a clothianidin water disperscible granule (using a 50% waterdisperscible granule, trade name: DANTOP) and a water-diluted liquid ofa lambda-cyhalothrin SC (using 100 g/L of a SC preparation, trade name:KAPATE ZEON, manufactured by SYNGENTA) was prepared so that the appliedamount of an effective component was the amount described in Table 1,and the furrow was spray-treated with the mixed liquid at a spray amountof 100 L/ha. Then, the furrow was seeded with corn (Zea Mays, varietyname: Kubrik) at intervals of 17 cm, and a soil on the side of thefurrow was gathered together to close the furrow. A seeding density ofcorn was 78000 seeds/ha. They were defined as example sections 1 and 2.

For comparison, a non-treatment section, which was seeded with corn inthe same manner as in the example sections except that a treatment witha chemical was not performed, was provided.

In any section, four places were arranged by a randomized block method,with one place having an area of 54 m² (18 m×3 m).

34 days after the treatment with a chemical, the total number of plantsof corn and the number of plants of corn damaged by Agriotes sotdidus ineach of the example sections 1 and 2 and the non-treatment section wereinvestigated, a damage plant rate was calculated in accordance with thefollowing equation, and then an average damage plants rate of the fourinvestigation sections was determined.

Damage plant rate (%)={(number of plants of corn damaged)/(total numberof plants of corn)}×100

The results are shown in Table 1.

TABLE 1 Application Name and amount application amount Damage plant ofclothianidin (g/ha) of the present rate (g/ha) compound (II) (%) Example25 Esfenvalerate 2.3 section 1 20  Example 25 Lambda-cyhalothrin 1.7section 2   7.5 Non-treatment 0 0 34.6 section

Example 2

In a glass bottle having a volume of 10 ml, 10 mg of esfenvalerate wasdissolved in 1.8 ml of acetone, and 2 g of diatomaceous earth finegrains (trade name: ISOLITE CG, manufactured by ISOLITE INSULATINGPRODUCTS CO., LTD.) was added to the glass bottle, and the glass bottlewas strongly shaken to obtain a 0.5% esfenvalerate granule.

A clothianidin granule (using a 0.7% granule, trade name: DantotsuGranule, manufactured by Sumitomo Chemical Company, Limited), athiamethoxam granule (using a 0.5% granule, trade name: Actara Granule5, manufactured by Syngenta Japan K. K.), an imidacloprid granule (usinga 1.0% granule, trade name: Admirer 1 Granule, manufactured by BayerCropScience K.K.) or a thiacloprid granule (using a 1.0% granule, tradename: BARIARD Box Granule, manufactured by Nihon Nohyaku Co., Ltd.) anda tefluthrin granule (using a 0.5% granule, trade name: Force Granule,manufactured by Syngenta Japan K.K.) or the above-mentionedesfenvalerate were mixed in the combination described in Table 2.

A plastic cup (diameter 7 cm) having a volume of 390 ml was filled witha soil, a furrow was formed to a depth of 3 cm from the soil surface,the prepared mixed granule was, respectively, applied in the chemicalamount described in Table 2, the furrow was seeded with corn (varietyname: Pioneer 32K61, hybrid variety) in an amount of one grain per cup,and a soil on the side of the furrow was gathered together to close thefurrow. Corn was grown in a usual green house.

10 days after seeding of corn, 10 insects of Rhopalosiphum padi werereleased in each cup. This is called a treatment section.

On the other hand, except that a mixed granule was not applied, corn wasgrown in a usual green house in the same manner as in the treatmentsection, and 10 insects of Rhopalosiphum padi were released. This iscalled a non-chemical-treatment section.

3 days after insect releasing, the number of Rhopalosiphum padi wasinvestigated, and a preventive value was calculated using the followingequation. The results are shown in Table 2.

preventive value=100×(A−B)/A

A: number of insects during investigation of non-chemical-treatmentsection

B: number of insects during investigation of treatment section

TABLE 2 The present The present Preventive compound (I) compound (II)value Example Clothianidin Tefluthrin 100 section 3 25 g a.i./ha 25 ga.i./ha Example Clothianidin Tefluthrin 100 section 4 25 g a.i./ha 100 ga.i./ha Example Clothianidin Tefluthrin 100 section 5 25 g a.i./ha 150 ga.i./ha Example Imidacloprid Tefluthrin 100 section 6 100 g a.i./ha 25 ga.i./ha Example Thiamethoxam Tefluthrin 100 section 7 100 g a.i./ha 50 ga.i./ha Example Thiamethoxam Esfenvalerate 100 section 8 150 g a.i./ha25 g a.i./ha Example Thiacloprid Tefluthrin 100 section 9 150 g a.i./ha25 g a.i./ha

Example 3

Aqueous solutions of a thiamethoxam water soluble granule (using a 10.0%preparation, trade name: Actara Water Soluble Granule, manufactured bySyngenta Japan K.K.), an imidacloprid water dispersible granule (using a50.0% preparation, trade name: Admire Water dispersible Granule,manufactured by Bayer CropScience K.K.) and a thiacloprid waterdispersible granule (using a 30.0% preparation, trade name: BariardWater Dispersible Granule, manufactured by Bayer CropScience K.K.) andaqueous solutions of an esfenvalerate emulsifiable concentrate (using 50g/L of an EC preparation, trade name: Sumialpha 5EC, manufactured byPhilagro), a lambda-cyhalothrin emulsifiable concentrate (using 25 g/Lof an EC preparation, trade name: KARATE 2.5EC, manufactured bySYNGENTA) and a cypermethrin emulsifiable concentrate (using 50 g/L ofan EC preparation, trade name: Cymbush 5EC, manufactured by SYNGENTA)were mixed so as to achieve the combination and chemical amountdescribed in Table 3, thereby preparing a liquid containing thechemicals.

A plastic cup (diameter 7 cm) having a volume of 390 ml was filled witha soil, a furrow was formed to a depth of 3 cm from the soil surface,the prepared liquid containing chemical was, respectively, applied inthe chemical amount described in Table 3, the furrow was seeded withcorn (variety name: Pioneer, hybrid variety) in an amount of one grainper cup, and a soil on the side of the furrow was gathered together toclose the furrow. Corn was grown in a usual green house.

10 days after seeding of corn, 10 insects of Rhopalosiphum padi werereleased in each cup. This is called a treatment section.

On the other hand, except that a liquid containing the chemical was notapplied, corn was grown in a usual green house in the same manner as inthe treatment section, and 10 insects of Rhopalosiphum padi werereleased. This is called a non-chemical-treatment section.

3 days after insect releasing, the number of Rhopalosiphum padi wasinvestigated, and a preventive value was calculated using the followingequation. The results are shown in Table 3.

preventive value=100×(A−B)/A

A: number of insects during investigation of non-chemical-treatmentsection

B: number of insects during investigation of treatment section

TABLE 3 The present The present Preventive compound (I) compound (II)value Example Imidacloprid Esfenvalerate 100 section 10 20 g a.i./ha 200g a.i./ha Example Imidacloprid Lambda-cyhalothrin 100 section 11 200 ga.i./ha 20 g a.i./ha Example Imidacloprid Cypermethrin 100 section 12 20g a.i./ha 200 g a.i./ha Example Thiamethoxam Lambda-cyhalothrin 100section 13 20 g a.i./ha 200 g a.i./ha Example Thiamethoxam Cypermethrin100 section 14 100 g a.i./ha 50 g a.i./ha Example ThiaclopridCypermethrin 100 section 15 200 g a.i./ha 20 g a.i./ha

Example 4

A chemical fertilizer (N:P:K=15:15:15) is applied to the soil surface ofa cultivated land at 300 kg/ha, and the cultivated land is then plowed.

7 days after fertilization, for suppressing generation of weeds, thesoil surface of the whole cultivated land is spray-treated with a mixedliquid containing thiencarbazone-methyl and isoxaflutole, each of whichbeing a herbicide, and cyprosulfamide which is a safener at 150 L/ha sothat the application amounts of thiencarbazone-methyl, isoxaflutole andcyprosulfamide are 9.2 g/ha, 23 g/ha and 15 g/ha, respectively.

21 days after fertilization, using a pneumatic seeder (disk furrowopener), a cultivated land is ditched at intervals of 75 cm to a depthof 5 cm from the soil surface, and a mixed granule of clothianidin andtefluthrin is applied to the furrow so as to achieve an applicationamount of 30 g/ha for clothianidin and 50 g/ha for tefluthrin. Afterapplication, the furrow is seeded with corn (Zea Mays: hybrid variety).The furrow is seeded at intervals of 20 cm using, as a seed of corn, onetreated with thiuram. A seeding density of corn is 70000 seeds/ha. Afterthe furrow is seeded with corn, a soil on the side of the furrow isgathered together to close the furrow. This is called a treatmentsection.

For comparison, the furrow is seeded with corn by the operation same asthat in the treatment section except that clothianidin and tefluthrinare not applied. This is called a non-treatment section.

In any section, four places are arranged by a randomized block method,with one place having an area of 45 m² (15 m×3 m).

17 days after application of clothianidin and tefluthrin, the number ofplants of corn germinated is investigated, with central two rows of fourrows of seeded furrows as an investigation section, for the treatmentsection and the non-treatment section. 165 days after application ofclothianidin and tefluthrin, the number of plants of corn lodged due todamage by Diabrotica virgifera virgifera and Agriotes lineatus in thefurrows of the treatment section and the non-treatment section, forwhich the number of plants of corn germinated is investigated, isinvestigated, a lodge rate is calculated in accordance with thefollowing equation, and then an average lodge rate for the fourinvestigation sections is determined.

Lodge rate (%)=[(plant number of corn lodged)/(plant number of corngerminated)]×100

As a result, the treatment section shows a low lodge rate as compared tothe non-treatment section, and is found to have reduced damage byharmful organisms in corn cultivation.

Example 5

A chemical fertilizer (N:P:K=15:15:15) is applied to the soil surface ofa cultivated land at 300 kg/ha, and the cultivated land is then plowed.

7 days after fertilization, for suppressing generation of weeds, thesoil surface of the whole cultivated land is spray-treated with a mixedliquid containing thiencarbazone-methyl and isoxaflutole, each of whichbeing a herbicide, and cyprosulfamide which is a safener at 150 L/ha sothat the application amounts of thiencarbazone-methyl, isoxaflutole andcyprosulfamide are 9.2 g/ha, 23 g/ha and 15 g/ha, respectively.

21 days after fertilization, using a pneumatic seeder (disk furrowopener) equipped with a power sprayer, a cultivated land is ditched atintervals of 75 cm to a depth of 3 cm from the soil surface, and atefluthrin granule is applied to the furrow such that the applicationamount of tefluthrin is 75 g/ha. After application, the furrow is seededwith corn (Zea Mays: hybrid variety). The furrow is seeded at intervalsof 20 cm using, as a seed of corn, one treated with thiuram. A seedingdensity of corn is 70000 seeds/ha. In parallel with seeding of corn, anaqueous suspension of imidacloprid is applied to the furrow such thatthe chemical is in direct contact with the seed. The furrow isspray-treated at 150 L/ha so that the application amount of imidaclopridis 100 g/ha, and then a soil on the side of the furrow is gatheredtogether to close the furrow. This is called a treatment section.

For comparison, the furrow is seeded with corn by the operation same asthat in the treatment section except that tefluthrin and imidaclopridare not applied. This is called a non-treatment section.

In any section, four places are arranged by a randomized block method,with one place having an area of 45 m² (15 m×3 m).

17 days after application of tefluthrin and imidacloprid, the number ofplants of corn germinated is investigated, with central two rows of fourrows of seeded furrows as an investigation section, for the treatmentsection and the non-treatment section. 165 days after application oftefluthrin and imidacloprid, the number of plants of corn lodged due todamage by Diabrotica virgifera virgifera and Agriotes lineatus in thefurrows of the treatment section and the non-treatment section, forwhich the number of plants of corn germinated is investigated, isinvestigated, a lodge rate is calculated in accordance with thefollowing equation, and then an average lodge rate for the fourinvestigation sections is determined.

Lodge rate (%)=[(plant number of corn lodged)/(plant number of corngerminated)]×100

As a result, the treatment section shows a low lodge rate as compared tothe non-treatment section, and is found to have reduced damage byharmful organisms in corn cultivation.

Example 6

Ammonium phosphate (N:P:K=12:52:0) and urea (N:P:K=46:0:0), each ofwhich being a fertilizer, are applied to the soil surface of acultivated land at 100 kg/ha and 260 kg/ha, respectively, and thecultivated land is then plowed.

In order to prevent generation of weeds, 28 days after fertilization,the whole cultivated land is spray-treated with a mixed agent (using 610g/kg water dispersible granule, trade name: MaisTer, manufactured byBayer CropScience) of foramsulfuron and an iodosulfuron-methyl-sodiumsalt, each of which being a herbicide, and a safener, isoxadifen-ethyl,at 0.15 L/ha in terms of an application amount of the preparation.

3 days after application of the preparation, using a pneumatic seeder(disk furrow opener) equipped with a power sprayer, a cultivated land isditched at intervals of 75 cm to a depth of 4 cm from the soil surface,and the furrow is seeded with corn (Zea Mays; hybrid variety). Thecultivated land is seeded at intervals of 20 cm using, as a corn seed,one treated with a mixed agent of metalaxyl-M and fludioxonil (tradename: Maxim XL, manufactured by Syngenta). A seeding density of corn is66667 seeds/ha. Then, the furrow is spray-treated with a mixed aqueoussuspension of tefluthrin and thiamethoxam at 125 L/ha so that theapplication amount is 50 g/ha for tefluthrin and 50 g/ha forthiamethoxam. This is called a treatment section.

For comparison, the furrow is seeded with corn by the operation same asthat in the treatment section except that tefluthrin and thiamethoxamare not applied. This is called a non-treatment section.

In any section, four places are arranged by a randomized block method,with one place having an area of 45 m² (15 m×3 m).

17 days after application of tefluthrin and thiamethoxam, the number ofplants of corn germinated is investigated, with central two rows of fourrows of seeded furrows as an investigation section, for the treatmentsection and the non-treatment section.

165 days after application of tefluthrin and thiamethoxam, the number ofplants of corn lodged due to damage by Diabrotica virgifera virgiferaand Agriotes lineatus in the furrows of the treatment section and thenon-treatment section, for which the number of plants of corn germinatedis investigated, is investigated, a lodge rate is calculated inaccordance with the following equation, and then an average lodge ratefor the four investigation sections is determined.

Lodge rate (%)=[(plant number of corn lodged)/(plant number of corngerminated)]×100

As a result, the treatment section shows a low lodge rate as compared tothe non-treatment section, and is found to have reduced damage byharmful organisms in corn cultivation.

Example 7

A chemical fertilizer (N:P:K=15:15:15) is applied to the soil surface ofa cultivated land at 300 kg/ha, and the cultivated land is then plowed.

7 days after fertilization, for suppressing generation of weeds, thesoil surface of the whole cultivated land is spray-treated with a mixedliquid containing thiencarbazone-methyl and isoxaflutole, each of whichbeing a herbicide, at 150 L/ha so that the application amounts ofthiencarbazone-methyl and isoxaflutole are 9.2 g/ha and 23 g/ha.

21 days after fertilization, using a pneumatic seeder (disk furrowopener), a cultivated land is ditched at intervals of 75 cm to a depthof 5 cm from the soil surface, and a mixed granule of clothianidin andtefluthrin is applied to the furrow so as to achieve an applicationamount of 30 g/ha for clothianidin and 50 g/ha for tefluthrin. Afterapplication, the furrow is seeded with corn (Zea Mays: hybrid variety).The furrow is seeded at intervals of 20 cm using, as a seed of corn, onetreated with thiuram and cyprosulfamide which is a safener. A seedingdensity of corn is 70000 seeds/ha. After the furrow is seeded with corn,a soil on the side of the furrow is gathered together to close thefurrow. This is called a treatment section.

For comparison, the furrow is seeded with corn by the operation same asthat in the treatment section except that clothianidin and tefluthrinare not applied. This is called a non-treatment section.

In any section, four places are arranged by a randomized block method,with one place having an area of 45 m² (15 m×3 m).

17 days after application of clothianidin and tefluthrin, the number ofplants of corn germinated is investigated, with central two rows of fourrows of seeded furrows as an investigation section, for the treatmentsection and the non-treatment section. 165 days after application ofclothianidin and tefluthrin, the number of plants of corn lodged due todamage by Diabrotica virgifera virgifera and Agriotes lineatus in thefurrows of the treatment section and the non-treatment section, forwhich the number of plants of corn germinated is investigated, isinvestigated, a lodge rate is calculated in accordance with thefollowing equation, and then an average lodge rate for the fourinvestigation sections is determined.

Lodge rate (%)=[(plant number of corn lodged)/(plant number of corngerminated)]×100

As a result, the treatment section shows a low lodge rate as compared tothe non-treatment section, and is found to have reduced damage byharmful organisms in corn cultivation.

Example 8

A chemical fertilizer (N:P:K=15:15:15) is applied to the soil surface ofa cultivated land at 300 kg/ha, and the cultivated land is then plowed.

7 days after fertilization, for suppressing generation of weeds, thesoil surface of the whole cultivated land is spray-treated with a mixedliquid containing thiencarbazone-methyl and isoxaflutole, each of whichbeing a herbicide, at 150 L/ha so that the application amounts ofthiencarbazone-methyl and isoxaflutole are 9.2 g/ha and 23 g/ha.

21 days after fertilization, using a pneumatic seeder (disk furrowopener) equipped with a power sprayer, a cultivated land is ditched atintervals of 75 cm to a depth of 3 cm from the soil surface, and atefluthrin granule is applied to the furrow such that the applicationamount of tefluthrin is 75 g/ha. After application, the furrow is seededwith corn (Zea Mays: hybrid variety). The furrow is seeded at intervalsof 20 cm using, as a seed of corn, one treated with thiuram. A seedingdensity of corn is 70000 seeds/ha. In parallel with seeding of corn, anaqueous suspension of imidacloprid and cyprosulfamide which is a safeneris applied to the furrow such that the chemical is in direct contactwith the seed. The furrow is spray-treated at 150 L/ha so that theapplication amounts of imidacloprid and cyprosulfamide are 100 g/ha and15 g/ha, and then a soil on the side of the furrow is gathered togetherto close the furrow. This is called a treatment section.

For comparison, the furrow is seeded with corn by the operation same asthat in the treatment section except that tefluthrin and imidaclopridare not applied. This is called a non-treatment section.

In any section, four places are arranged by a randomized block method,with one place having an area of 45 m² (15 m×3 m).

17 days after application of tefluthrin and imidacloprid, the number ofplants of corn germinated is investigated, with central two rows of fourrows of seeded furrows as an investigation section, for the treatmentsection and the non-treatment section. 165 days after application oftefluthrin and imidacloprid, the number of plants of corn lodged due todamage by Diabrotica virgifera virgifera and Agriotes lineatus in thefurrows of the treatment section and the non-treatment section, forwhich the number of plants of corn germinated is investigated, isinvestigated, a lodge rate is calculated in accordance with thefollowing equation, and then an average lodge rate for the fourinvestigation sections is determined.

Lodge rate (%)=[(plant number of corn lodged)/(plant number of corngerminated)]×100

As a result, the treatment section shows a low lodge rate as compared tothe non-treatment section, and is found to have reduced damage byharmful organisms in corn cultivation.

Example 9

A land was ditched at intervals of 80 cm, a predetermined amount of awater-diluted liquid of an esfenvalerate emulsifiable concentrate (using25 g/L of an EC preparation, trade name: Sumialpha 2.5 EC, manufacturedby Philagro) or a water-diluted liquid of a lambda-cyhalothrin SC (using100 g/L of a SC preparation, trade name: KAPATE ZEON, manufactured bySYNGENTA) was prepared so that the applied amount of an effectivecomponent was the amount described in Table 4, and the furrow wasspray-treated with the liquid at a spray amount of 100 L/ha. Then, thefurrow was seeded with corn (Zea Mays, variety name: Kubrik), and a soilon the side of the furrow was gathered together to close the furrow. Aseeding density of corn was 87500 seeds/ha. They were defined as examplesections 16 and 17.

For comparison, a non-treatment section, which was seeded with corn inthe same manner as in the example sections except that a treatment witha chemical was not performed, was provided.

In any section, four places were arranged by a randomized block method,with one place having an area of 38.4 m² (12 m×3.2 m) and other threeplaces having an 32 m² (10 m×3.2 m).

34 days after the treatment with a chemical, the number of plants ofcorn grown in each of the example sections 16 and 17 and thenon-treatment section were investigated, a mortality of plants of corndied because of the damage by Agriotes spp. was calculated in accordancewith the following equation, and then an average mortality of the fourinvestigation sections was determined.

Mortality (%)={(number of corns seeded)−(number of plants of corngrown)/(number of corns seeded)}×100

The results are shown in Table 4.

TABLE 4 Name and application amount Average (g/ha) of the presentmortality compound (II) (%) Example Esfenvalerate 4.85 section 16 50Example Lambda-cyhalothrin 3.35 section 17 50 Non-treatment  0 16.35section

Example 10

A chemical fertilizer (N:P:K=15:15:15) is applied to the soil surface ofa cultivated land at 300 kg/ha, and the cultivated land is then plowed.

7 days after fertilization, for suppressing generation of weeds, thesoil surface of the whole cultivated land is spray-treated with a mixedliquid containing thiencarbazone-methyl and isoxaflutole, each of whichbeing a herbicide, and cyprosulfamide which is a safener at 150 L/ha sothat the application amounts of thiencarbazone-methyl, isoxaflutole andcyprosulfamide are 9.2 g/ha, 23 g/ha and 15 g/ha, respectively.

21 days after fertilization, using a pneumatic seeder (disk furrowopener), a cultivated land is ditched at intervals of 75 cm to a depthof 5 cm from the soil surface, and a water-diluted liquid of anesfenvalerate emulsifiable concentrate (using 25 g/L of an ECpreparation, trade name: Sumialpha 2.5 EC, manufactured by Philagro) isapplied to the furrow so as to achieve an application amount of 100 g/hafor esfenvalerate. After application, the furrow is seeded with corn(Zea Mays: hybrid variety). The furrow is seeded at intervals of 20 cmusing, as a seed of corn, one treated with thiuram. A seeding density ofcorn is 70000 seeds/ha. After the furrow is seeded with corn, a soil onthe side of the furrow is gathered together to close the furrow. This iscalled a treatment section.

For comparison, the furrow is seeded with corn by the operation same asthat in the treatment section except that esfenvalerate is not applied.This is called a non-treatment section.

In any section, four places are arranged by a randomized block method,with one place having an area of 45 m² (15 m×3 m). 17 days afterapplication of esfenvalerate, the number of plants of corn germinated isinvestigated, with central two rows of four rows of seeded furrows as aninvestigation section, for the treatment section and the non-treatmentsection. 165 days after application of esfenvalerate, the number ofplants of corn lodged due to damage by Diabrotica virgifera virgiferaand Agriotes lineatus in the furrows of the treatment section and thenon-treatment section, for which the number of plants of corn germinatedis investigated, is investigated, a lodge rate is calculated inaccordance with the following equation, and then an average lodge ratefor the four investigation sections is determined.

Lodge rate (%)=[(plant number of corn lodged)/(plant number of corngerminated)]×100

As a result, the treatment section shows a low lodge rate as compared tothe non-treatment section, and is found to have reduced damage byharmful organisms in corn cultivation.

Example 11

A chemical fertilizer (N:P:K=15:15:15) is applied to the soil surface ofa cultivated land at 300 kg/ha, and the cultivated land is then plowed.

7 days after fertilization, for suppressing generation of weeds, thesoil surface of the whole cultivated land is spray-treated with a mixedliquid containing thiencarbazone-methyl and isoxaflutole, each of whichbeing a herbicide, and cyprosulfamide which is a safener at 150 L/ha sothat the application amounts of thiencarbazone-methyl, isoxaflutole andcyprosulfamide are 9.2 g/ha, 23 g/ha and 15 g/ha, respectively.

21 days after fertilization, using a pneumatic seeder (disk furrowopener), a cultivated land is ditched at intervals of 75 cm to a depthof 5 cm from the soil surface, and a water-diluted liquid of alambda-cyhalothrin SC (using 100 g/L of a SC preparation, trade name:KAPATE ZEON, manufactured by SYNGENTA) is applied to the furrow suchthat the application amount of lambda-cyhalothrin is 100 g/ha. Afterapplication, the furrow is seeded with corn (Zea Mays: hybrid variety).The furrow is seeded at intervals of 20 cm using, as a seed of corn, onetreated with thiuram. A seeding density of corn is 70000 seeds/ha. Afterthe furrow is seeded with corn, a soil on the side of the furrow isgathered together to close the furrow. This is called a treatmentsection.

For comparison, the furrow is seeded with corn by the operation same asthat in the treatment section except that lambda-cyhalothrin is notapplied. This is called a non-treatment section.

In any section, four places are arranged by a randomized block method,with one place having an area of 45 m² (15 m×3 m).

17 days after application of lambda-cyhalothrin, the number of plants ofcorn germinated is investigated, with central two rows of four rows ofseeded furrows as an investigation section, for the treatment sectionand the non-treatment section. 165 days after application oflambda-cyhalothrin, the number of plants of corn lodged due to damage byDiabrotica virgifera virgifera and Agriotes lineatus in the furrows ofthe treatment section and the non-treatment section, for which thenumber of plants of corn germinated is investigated, is investigated, alodge rate is calculated in accordance with the following equation, andthen an average lodge rate for the four investigation sections isdetermined.

Lodge rate (%)=[(plant number of corn lodged)/(plant number of corngerminated)]×100

As a result, the treatment section shows a low lodge rate as compared tothe non-treatment section, and is found to have reduced damage byharmful organisms in corn cultivation.

1. A method for reducing damage by harmful organisms in corncultivation, the method comprising the steps of: A) making a furrow in acultivated land; B) seeding with corn the furrow formed in the foregoingstep; C) applying to the furrow one or more selected from thebelow-mentioned compound group (II); and D) closing the furrow,(compound group (II): group consisting of bifenthrin, bioresmethrin,deltamethrin, bioallethrin, ethofenprox, fenpropathrin, cypermethrin,alpha-cypermethrin, zeta-cypermethrin, fenvalerate, esfenvalerate,cyfluthrin, beta-cyfluthrin, alpha-cypermethrin, tralomethrin,fluvalinate, permethrin, lambda-cyhalothrin, flucythrinate andtefluthrin), wherein the step of applying one or more selected from thecompound group (II) is a step of applying a composition containing oneor more selected from the compound group (II), and wherein thecomposition containing one or more selected from the compound group (II)is an aqueous dispersion or aqueous solution containing one or moreselected from the compound group (II).
 2. The method according claim 1,wherein the aqueous dispersion or aqueous solution is an aqueousdispersion or aqueous solution obtained by dispersing or dissolving inwater a water soluble powder, a wettable powder, a water dispersiblegranule, a soluble concentrate, a microcapsule, an emulsifiableconcentrate, a concentrated emulsion, a microemulsion, a suspoemulsion,an oil miscible liquid, a suspension concentrate or a dry flowable whichcontains one or more selected from the compound group (II).
 3. Themethod according to claim 1, wherein the land is ditched to a depth of 1to 10 cm.
 4. The method according to claim 1, wherein making the furrowis performed using a disk furrow opener.
 5. The method according toclaim 1, wherein seeding is performed using a pneumatic seeder.